Training Lead I

hace 2 semanas

Alajuela, Alajuela, Costa Rica Abbott Laboratories A tiempo completo

_MAIN PURPOSE OF ROLE_


Under supervision of Training/Production Supervisor, Training Sr will be on charge to coordinate and follow up all training related activities in the production lines under responsibility, it includes but is not limited to: skill training and progress report, evaluate training, certify operators and other activities required to ensure permanent regulatory compliance of Training system.

**_
MAIN RESPONSIBILITIES_**- Develop area trainers and coordinate workload of training plans.

  • Control training resources as workstations, materials, tools and fixtures required to perform training.
  • Understand production training requirements, propose and track training plans accordingly.
  • Monitor the performance of trainees ensuring that training requirements are met.
  • Maintain physical records and LMS uptodate to follow up any issue with data traceability.
  • Administer LMS to support quality investigations, assign/remove audiences and other tasks as needed.
  • Collaborate in the preparation of documentation and remediation activities related to external/internal audits. Perform audits as required.
  • Participate in functional team meetings and start up meetings as required.
  • Gather information to fulfill Training system metrics and submit the monthly report.
  • Partners with engineering and/or operations to support the review and update of training system as appropriate.
  • Role model on Abbott policies and compliance culture
  • Capable to develop healthy yet challenging relations with coworkers where negotiation, transparency, integrity and positive confrontation are observable behaviors.
  • Assists supervisor with other tasks as necessary.

_ QUALIFICATIONS_

_ Education_
High school degree

_ Experience/Background_

Experience
3 years of experience within a trainer or coordination role

_ Experience Details_

  • Capable to transfer knowledge/skills from person to person with minimum deviation from current Manufacturing procedure.
  • Must have the ability to read and interpret written documentation to build own criteria on the best way to accomplish regulatory and operative tasks.
  • Basic Proficiency in MS office platform: Excel, outlook, power point.
  • Basic knowledge on Abbott QMS or Medical devices regulation.
  • Previous experience in a manufacturing environment on positions with activity coordination, provide feedback and demonstrated ability to influence trainers and peers, capable to manage up as needed.

_ SHIFT TB_

_ Language Proficiency_

  • Basis English level / Required

_ Preferred Qualifications & Education _

  • Basic knowledge of Labor laws applicable to manufacturing environment.
  • Technical Studies on engineering or administration are highly desirable.
  • External courses or certifications on QSRs, GMPs, Lean, technical writing.

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